Colon Cancer: Gene >> NPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32786260:32786260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541G>T
AA Mutation	p.Arg514Met(p.R514M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32786263:32786263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32712392:32712392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>A
AA Mutation	p.Asp206Asn(p.D206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32782990:32782990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41270319
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463Gln(p.R463Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32786307:32786307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142228984
CDS Mutation	c.1588C>T
AA Mutation	p.Arg530Trp(p.R530W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32712372:32712372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596G>A
AA Mutation	p.Arg199His(p.R199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32712188:32712188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412T>C
AA Mutation	p.Tyr138His(p.Y138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32786328:32786328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609C>A
AA Mutation	p.His537Asn(p.H537N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32782896:32782896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1294A>G
AA Mutation	p.Ile432Val(p.I432V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32712018:32712018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242G>A
AA Mutation	p.Arg81His(p.R81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32711781:32711781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5C>T
AA Mutation	p.Pro2Leu(p.P2L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265074
Start	32774734:32774734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147308580
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265074
Start	32738895:32738895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760115815
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265074
Start	32712199:32712199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000265074
Start	32724711:32724711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783T>A
AA Mutation	p.Cys261Ter(p.C261*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000265074
Start	32780760:32780760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774338813
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Ter(p.R412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265074
Start	32782980:32782980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>A
AA Mutation	p.Asp460Asn(p.D460N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265074
Start	32712220:32712220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265074
Start	32738874:32738874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903A>C
Mutation Classification	Silent
Feature Type	Transcript